Showing posts with label Bill Deagle MD. Show all posts
Showing posts with label Bill Deagle MD. Show all posts

Monday, April 27, 2009

FLU: Recombinant Preparedness Alert

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Use the SEARCH window to locate the many articles we have posted on flu and flu vaccines at Natural Health News


Swine Flu Epidemic & Avianized Flu Pandemic
Dr Bill Deagle MD DABFP AAEM A4M
4-26-9
Zoonotic Vectors of Swine and Avian Flu

The swine flu is common in the agribusiness, and antibodies to swine flu are present in 20% of vetenarians and 5% of pig farm workes, and rarely kills pigs. However, this swine flu that has presented in Mexico, Texas, California, Queens NYC, London, Italy, etc. has genes of swine, avian, human, and asian flu.

This is without any doubt a pandemic flu with a current case fatality estimated at
10% plus, and rapidly is leaping across North America and to Europe.

Since 1997, the H5N1 flu has spread to all continents. Genetics showed that six strains had high pathogenic case fatality rates in the range of 70% average from 25% to 100% case fatality rates in humans, with some clusters of human to human spread, with close physical contact.

Defiencies in two amino acids needed to allow rapid attachment to human cells was found in all strains, but can be acquired by recombinants with H9N2 or H7N3 or H3N2 etc. endemic human stains that can also coinfect pigs, birds, agricultural animals, and animals in the wild.

Until fall 2008, the avian flu did not optimally replicate unless it was at 106 degrees or higher, but now it has acquired the capacity to replicate easily at 98.6 Farhenheit.

Drug resistance to Amantadine, Tamiflu also are the predominant strains. The current swine flu is analagous to a early 20th century steamer trunk, with stickers showing the visited countries and coastal cities. It has stamps from Asia, North America, Avian, Swine and Human genetics. This is a "Lab Creation".

Now, we must understand that this virus is behaving as if it is more lethal per case that usual flu, and can recombine in pigs, wild and domestic birds, and other animals and can thus acquire PB2 deletions, NS1 gene polymorphisms, and the polybasic six amino acids that allow it to grow in brain and CNS as well as any other target organ in human and animal hosts.

The NS1 deletion of four amino acids bypasses IL4, and thus is much more lethal with massive cytokine release at end stages. Because Avian H5N1 and the 1918 Swine Flu targeted young healthy people, the release of cytokines was more violent in the most healthy.

This first wave is likely to recombine and after Phase 1 gene to population insertion, Phase 2 will result in new superstrains with additional genetic polymorphisms allow transfer efficiently to humans. Phase 2 is the bioreactor phase.

In the emergent or Phase 3, new viral Clades of Swine /Avian hybrids will then have more efficient spreading and higher spontaneous lethality.

WHO Watchdog and Author of Pandemic FLU!
Human Life International invited Dr Bill Deagle MD to speak, March 1997, to the International Board of Doctors and Scientists. After a two hour talk, the board sat me down for a presentation of a foot of documents. Included were three distinct biological programs. The first was a plasmid anti-HCG contaminated Tetanus Vaccine, to cause first trimester sterility by spontaneous induced miscarriage in the target populations of Subsharan Africa, Phillipines, and other target WHO UN high density population countries. The second program was the US Special Virus Project, with mycoplasma RNA oncogenic viruses to cause immune failure, and premature death. It was knows as the AIDS syndrome, and was a recombinant of Visna, Green Monkey and Feline leukemia retro-RNA viruses carried by host mycobacteria. Most important as the large packet of documents on the Avian Flu Project, funded by the Rothchilds and oversean by the WHO and UN. They were in process of obtaining gene fragments from deceased whalers in Alaska with the CDC and Natl Institute of Allergy and Infectious Disease, supercomputer remodeled and bioengineered resurrection of the 1918 Swine Flu. They planned to insert into the genome Avian genes and spray into Asian bird populations, which would later be a gene pool when spread was complete to all continents for a new Swine-Avian Flu Pandemic.

We now see the H1N1 flu in Mexico, Canada, UK, Italy, USA and perhaps other locations, rapidly evolving. This wave is quite lethal, but with the H5N1 genetics in the wild, it is likely to come in future waves with yet more lethal genes and more rapid spread. Certainly, in the next 7 days, the presence in multiple countries, US Pandemic Flu Alert, WHO raised from 3rd to 4th level, and the pronouncements for a decade plus of coming Pandemic Flu, this was totally a UN WHO plot to release a virus that would cull the human herd.

This is - Global 2000, NSSM 1974 population threat alerts, 1996 UN Population control documents - all calling for massive reduction in World Human Populations. Last week, the UK Prime Minister Gordon Brown called for a reduction from 60 to 30 million.

Sunday, December 7, 2008

Yes, Aspartame is TOXIC and don't think otherwise

UPDATE: Dec 18
Please read this important article by Bill Deagle, MD if you need more facts about the toxicity of aspartame, yet another substance originally approved as an insecticide -
ASPARTAME IS NEUROTOXIC

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This morning I received an anonymous post in response to the many articles I have posted both on my original website and Natural Health News. The post came with a signature of John E. Garst.

I was not willing to post the comment because it is submitted anonymously, which is the antithesis of our policy. We will post comments if they are submitted with your name and request it be posted without your name, and it is salient to the topic.

Whoever the Garst fellow is I found his attack on my background offensive as he states the following:
John E. Garst, Ph.D. (Medicinal Chemistry, Pharmacology, Toxicology, and Nutrition)
(FYI, I have absolutely no financial or biasing connection with the aspartame, the soft drink or related industries. However, I am just tired of people who have no understanding of the the sciences of pharmacology and toxicology trying to pass judgment by hearsay on something that they know nothing about.)

I have an extensive understanding of pharmacology, toxicology, and nutrition, as well as human physiology, biochemistry and medicine.
Obviously the sender failed to read ABOUT....

Aspartame is toxic, it is an insecticide. If you want to ingest insecticide, just like Splenda as well, then do so at your own risk.

And if you don't want insecticides in the food you purchase or ingest I'd encourage you to write you Member of Congress and demand it be taken off the market.

However if you want the science, please read on.
ASPARTAME FLACK TRIES TO MISLEAD NEW MEXICO LEGISLATURE

John Garst brags that he played a major role in obliterating efforts to ban aspartame in 06. Hes trying to do it again by bombarding legislators with complicated lingo only a biochemist can comprehend. Its a vacuous bluff with hot air said James Bowen MD. who is a physician, surgeon, biochemist, and an aspartame victim with Lou Gehrigs.

New Mexico lawmakers are expected to take Garth's word for it and do what he wants. This last-minute blast is an ambush in bad faith, like yelling fire in a crowded theater so the legislature will run for the exits. Garst wants a stampede!

Good faith requires him to come forward in time for his assertions to be examined. But then he would be exposed. With no time for deliberation the legislators are expected to just accept his say-so.

At the say-so level: R G Walton M.D. Chairman, Center for Behavioral Medicine at NE Ohio College of Medicine analyzed 92 peer-reviewed studies not funded by aspartame industry. 92% found PROBLEMS!

There were also 74, sponsored by NutraSweet, which said its safe as rain. Dr. Walton concluded Serious questions have been raised about the reliability of industry-sponsored studies of the safety of synthetic chemicals. Aspartame, in particular, has been the focus of significant ongoing controversy Walton named numerous adverse clinical events including seizures, mood disorders, headaches and brain tumors.

In 95 the FDA listed 92 reactions from 10,000 volunteered complaints, including death.

H. J. Roberts, M.D., FACP a diabetic specialist has produced 20 books and his first text on medical diagnosis was used by 60,000 doctors to prepare for their Board examinations. In his response to Garst's allegation that aspartame sensitivity reflects folate deficiency, he wrote to the members of the New Mexico Legislature:

You have received correspondence concerning folate deficiency as the purported cause of aspartame disease. While folate plays a role in the metabolism of methanol (methyl alcohol), the severity and widespread nature of reactions to aspartame products suggest that this assertion must be tempered by the following:

*The methyl alcohol in aspartame is FREE (rarely found as such in nature.)

*The assertion that methanol concentrations never are very high after aspartame ingestion is erroneous. I devoted an entire chapter to methanol toxicity in my text, Aspartame Disease: An Ignored Epidemic (pp 668-685), and show in Figure XXI-1 the dose-related blood levels of methanollasting 8 or more hours.

*The assertion that many New Mexicans suffer from a folate deficiency is challenged. While I discussed such a theoretical deficiency in my text, there is no evidence that folate deficiency is widespread among Americans. For example, a Mayo Clinic study involving thousands of blood assays concluded that it was rare. Garst ignores the major roles of phenylalanine and aspartic acid in aspartame disease.

Enormous effort has gone into this constructive attempt to ban aspartame products. I believe that it constitutes an imminent health hazard for New Mexicans. You are to be congratulated for coming this far in the face of severe corporate resistance.

H. J. Roberts, M.D., FACP, FCCP

Dr. Maria Alemany, Departament du Nutricio I Bromatologia, Facultat de Biologia, Universitat de Barcelona, who was the researcher for the damning Trocho Study wrote that he was deeply insulted by Garsts propaganda. Remember that Dr. Alemanys study proved the formaldehyde converted from the free methyl alcohol embalms living tissue and damages DNA. As we know when you damage DNA you can destroy humanity. So concerned for the public was Dr. Alemany that after his study he reported it to the authorities. He told me personally that he was concerned aspartame could kill millions and I said has killed millions. After all aspartame can trigger all sorts of neurodegenerative diseases and tumors and can precipitate diabetes. Even the FDA found many types of tumors and brain cancer on original studies and the Ramazzini Study in 2005 confirmed FDA findings reporting the study showed aspartame to be a multipotential carcinogen. Dr. Alemany is a hero to the world and proved beyond a shadow of doubt what aspartame experts believed for years.

Dr. Alemany said: First, Garst suggests that perhaps aspartame just affects people with a metabolic deficit. If that were the case (I doubt it, deficits may just enhance the effect of aspartame), why then has it not been studied? In the case of cyclamate, the ban on its use is based on the deleterious effects on only a fraction of the population

Second. Dr. Garst accepts that aspartame yields formaldehyde... then, why not give formaldehyde to the people to help them synthesize methyl groups? Did I understood well (after speaking of the double helix which has very little to do here unless for the binding of formaldehyde to its strands to induce mutation) that Dr. Garst suggests that aspartame may be beneficial because its derived formaldehyde may supply one-carbon units for methylations through the folate pathway? If that were the case, why not get the FDA approval for aspartame as a drug/vitamin substitute? This is an outright fallacy (or better said bull-manure).

Third. Please, not again the tale of the methyl-esters of pectins! It has been proved to nausea that most of the methyl-alcohol esters of uronic acids remain esterified through intestinal passage, and that freed in the large intestine by the action of the flora is majoritarily and keenly used by these microbes for their profit. The remaining methyl alcohol leaving the intestine is largely detoxified by the liver (this is a physiological mechanism well known and proved effective for millennia). Aspartame, however, is not fully hydrolyzed in the intestine, being absorbed in part intact. After the intestine-portal vein-liver trap is surpassed, the body protection against methanol wanes, and the tiny liberation of methanol in tissues yields little amounts of formaldehyde that cause serious damage, precisely because it behaves very differently from the natural products methanol. Even in cases of wood-alcohol (methanol) intoxication, the liver helps to stem the overflow of toxic. Methanol inhalation or injection is much more dangerous, because it goes directly into the bloodstream and tissues jumping the liver barrier. This is explained in elementary physiology and biochemistry courses, it is unbelievable that this is maintained as a "serious" scientific position by somebody that got a PhD, unless this is not a discourse of science but of economy.

Theories are nice, but have to be proved true. The one Dr. Garst exposes here is that maintained by pro-aspartame fellows for decades. This is how they explained the incorporation of aspartame label into protein and DNA in the earliest experiments on aspartame using tracers that were published (none was published by this group thereafter). This theory fits very well with the story of a harmless aspartame, but it has been proven untrue. We did it, and this is why our study was so damaging. If the theory recycled by Dr. Garst were true, then, the carbon of the methyl alcohol of aspartame would enter the one-carbon path mediated by tetrahydrofolate, this can be done via formaldehyde or via formate. These one-carbon units may be processed (depending on demand) to methyl groups, such as those found in carnitine, thymine and methionine (the only amino acid that can get back methyl groups in mammals), thus explaining the presence of label in protein (methionine) or DNA (thymine). We gave labeled aspartame to rats, and got their DNA and protein from a number of tissues, and found large proportions of label. So far no differences with the Aspartame-lovers theory. However, we hydrolyzed the protein and DNA and looked for label in thymine in DNA and methionine in protein. We found none. Instead, the label was in unknown spots in the chromatograms, which plainly indicates that the incorporation of label into DNA and protein was NOT through the incorporation of methyl groups, i.e. the one-carbon folate pathway. Other ways of label incorporation should explain the attachment of the label. The most logical explanation (justified by innumerable studies that show that formaldehyde attaches to protein and other molecules) was that aspartame-derived formaldehyde was chemically bound to protein and DNA, inactivating (embalming, in fact) proteins and altering DNA structure causing mutations.

The experimental studies show that the theory is faulty. No counter-experiments were published showing our possible "errors", nor the theory of folate pathway incorporation has been proved experimentally (it is fairly easy to demonstrate, it only needs to be true, however). This is why I felt insulted. It is an insult to the intelligence of anybody with even a thin varnish of scientific knowledge to discard proven facts and stick to self-fulfilling harebrained theories. If what the aspartame lovers say about the fate of aspartame carbon is true, why nobody has proved it experimentally? It is easy to carry out and much less expensive than hiring lawyers to defend bad science with top dollar legal expertise

I used as heading the famous initial words of the second Catilinary by Cicero, which I remember from my early high-school Latin. Since probably most Americans were lucky enough not to study Latin when 10-11 years old, I provide an approximate translation: "Up to when do you, Catilina, will abuse our patience?", substitute Catilina for the present aspartame producers and probably it fits very well the picture.
Good luck on the banning of this menace to our collective health.
Best regards,
--------------------------
Dr. Maria Alemany
Departament de Nutrici i Bromatologia
Facultat de Biologia, Universitat de Barcelona
Av. Diagonal, 645
08028 Barcelona. Espanya / Espaa / Spain

Today in Dr. Roberts medical text there is a page on pre-embalming thanks to the work of the courageous Dr. Maria Alemany
--------------------------

Dr. James Bowen was extremely upset that John Garst tried to deceive the legislature, especially the day before the discussion and said, This is a brazen attempt to violate every due process procedure with respect to all scientific and legal hearings.. Dr. Garth's ambush is only an attempt to win against the health and welfare of the people of New Mexico, by unlawful and unscientific ambush and by utilizing brazen pseudo science lying.

He hopes to impress by using impressive Big Words from science! This is merely science trash I will mention one case of his falsity: abuse of science and scientific process. Dr. Garst says that the folate issue is one reason not to disturb the present commerce of aspartame. This causes a highly synergized form in human metabolism, obligatory: methanol to formaldehyde to formic acid to carbon monoxide toxic axis! Molecule for molecule, the deadly formic acid congener (formate) from aspartame metabolism consumes (molecule per molecule) one molecule of folic acid (folate) to eliminate the formate without creating subsequent carbon monoxide poisoning.

Aspartame has caused many years of folate iatrogenic deficiency, already causing many human illness epidemics, fetal deformities. When in l984 I called the FDA about this, because they had concurrent with their licensure of aspartame, abandoned their 50 year standard of folic acid ingestion by pregnant women (1 mg), leading to grievous fetal defects, they like Dr. Garst lied their way out saying: We have already checked all that out. There just aren't any problems at all. But neural tube, bladder defects and cardiac deformities escalated within our newborn population victimized by aspartame. Birth defects are a major epidemic caused by aspartame, with full protection and avid cooperation from the US FDA. James Bowen, M.D.

Mark Gold of the Aspartame Toxicity Center says this short document answers all of the aspartame industrys claims about aspartame and formaldehyde poisoning: http://www.holisticmed.com/aspartame/abuse/methanol.html

Dr. John Garst is a Ph.D and its obvious he knows he is publishing false information. His modus operandi is to use his credentials to deceive others because he cant debate true experts who can easily take apart his nonsense.

The New Mexico legislature has better sense to even consider Garst's claptrap. Aspartame manufacturers must sit up at night thinking of ways to deceive. Families all over the world have been destroyed by this poison causing male sexual dysfunction, cancer and diabetes and sudden death. Enough is enough. Aspartame must be banned from the planet to save the human race.

Dr. Betty Martini, D.Hum, Founder
Mission Possible International
9270 River Club Parkway
Duluth, Georgia 30097
770 242-2599
www.wnho.net and http://www.dorway.com
Aspartame Toxicity Center, http://www.holisticmed.com/aspartame
Aspartame Information List, http://www.mpwhi.com
Aspartame Documentary: Sweet Misery: A Poisoned World

 
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